Comparisonoflysismethods

Comparison of lysis methodsSonicationmost efficient method of cell fractionationproblem: heat build up which can denature proteins (proportionate to length of sonication)precaution: do on ice and sonicate intermittantlymaterial: ultrasonication bath or rodsHomogenisationbest for animal tissue; less suitable for cellsprecaution: do on ice to reduce heat build-up and denaturationmaterial: drills (polytron), pestle/tube......阅读全文

Comparison-of-lysis-methods

Comparison of lysis methodsSonicationmost efficient method of cell fractionationproblem: heat build up which can denature proteins (proportionate to l

Cell-and-tissue-lysis-hub

This page should point you to the many different general and lab-specific protocols describing tissue and cell lysis and serve as forum for comparison

Saponin-Lysis-of-RBCs

CuratorsJingyang Chen, Seattle Biomedical Research Institute, 307 Westlake Ave N, Suite 500, Seattle, WA, 98109, USA. jingyang.chen@sbri.orgAnyone sho

Urea-Lysis-Protocol

Urea lysis buffer            9M Urea, 2.5mM EDTA, 2.5mM EGTA, 1% DTE, 4% CHAPS            make 10ml and aliquot 10x1ml, freeze at -70°C Lysate prepara

Comparison-of-Beta-oxidation-in-mitochondria-and-peroxisomes-andglyoxysomes

In addition to the beta-oxidation of fatty acids in mitochondria, animal cells carry out beta-oxidation in another organelle, the peroxisome. Although

Red-Blood-Cell-Lysis-Protocols

实验概要BioLegend’s  Red Blood Cell (RBC) Lysis Buffer (Cat. No. 420301) has been designed,  formulated, and tested to ensure optimal lysis of RBCs in sin

Sauer:Lysing-E.-coli-with-Lysozymes

Getting The Most Out Of Your BugsNative lysis is a staple protocol in practically every biochemistry lab, yet there is significant variability in the

Comparison-of-Enzymatic-and-NonEnzymatic-Means1

Comparison of Enzymatic and Non-Enzymatic Means of Dissociating Adherent Monolayers of Mesenchymal Stem CellsThe dissociation of adherent mesenchymal

Comparison-of-Enzymatic-and-NonEnzymatic-Means3

MTT Assay on Reattached CellsAs seen in Fig.  2 , the proportion of viable MSC that re-attached was significantly higher (p  = 0.0004) upon dissociati

Comparison-of-Enzymatic-and-NonEnzymatic-Means2

MTT Assay on Reattached CellsMSC were seeded in 12-well cell culture dishes with 5.0 × 104 cells per well (≈4.8 cm2). After 5 to 6 days of culture, co

Preparation-of-Plasmid-DNA-by-Alkaline-Lysis-with-SDS:-Maxipreparation

实验概要Plasmid DNA is isolated from large-scale (500 ml) bacterial cultures by treatment with alkali and SDS.主要试剂Buffers and SolutionsAlkaline lysis solu

Preparation-of-Plasmid-DNA-by-Alkaline-Lysis-with-SDS:-Minipreparation

实验概要Plasmid DNA is isolated from small-scale (1-2 ml) bacterial cultures by treatment with alkali and SDS.主要试剂Buffers and Solutions:    Alkaline lysis

Staining-Methods-for-cell

death Z. Xia 10/2/95The simplest way: trypan blue. Dead cells stain blueNon-fixed cells: FDA(fluorescein diacetate)-green, alive cells; P.I. (propidiu

Jacobs:Protocol-Total-Protein-Isolation-Using-RIPA-Lysis-Buffer

MaterialsRIPA buffer (RIPA buffer enables the extraction of cytoplasmic, membrane and nuclear proteins and is compatible with many applications, inclu

红细胞裂解液(RBC-Lysis-Buffer,10×)-操作步骤

、组织细胞样本的常规操作1、制备细胞悬液: 新鲜组织经过胰蛋白酶或胶原酶等消化处理,通过适当方法制备成细胞悬液,离心弃上清。2、裂解: 加入1×RBC Lysis Buffer,轻柔吹打混匀,裂解1~2min。 3、离心,弃红色上清。本步骤亦可在室温下操作。4、如果发现红细胞裂解不完全,可以重复上述

Analysis-and-Reconstitution-of-Phycobiliproteins:-Methods-for-the-...

Analysis and Reconstitution of Phycobiliproteins: Methods for the Characterization of Bilin Attachment ReactionsPhycobiliproteins are a homologous fam

Plant-Genome-Annotation-Methods

Annotation of plant genomic sequences can be separated into structural and functional annotation. Structural annotation is the foundation of all g

Basic-Methods-of-Culturing-Drosophila

实验概要Basic Methods of Culturing Drosophila实验步骤Stockkeeping1. Mechanics        Most stocks can be successfully cultured by periodic mass transfer of a

General-Laboratory-Methods-for-Tetrapyrroles

There are thousands of porphyrins and metalloporphyrins, and hundreds of new derivatives appear each year. This variety arises because the cyclic

Methods-for-Xylem-Sap-Collection

Xylem and phloem are essential for the exchange of solutes and signals among organs of land plants. The synergy of both enables the transport and

Staining-Methods-for-cell-death

The simplest way: trypan blue. Dead cells stain blueNon-fixed cells: FDA(fluorescein diacetate)-green, alive cells; P.I. (propidium iodide)-red, dead

红细胞裂解液(RBC-Lysis-Buffer,10×)使用说明

红细胞裂解液(RBC Lysis Buffer,10×)简介在生物科研领域,经常需要去除红细胞。去除红细胞的方法有多种,如ACK Lysis Buffer、Tris-氯化铵红细胞裂解液、Gey's Lysis Buffer。红细胞裂解液(Red Blood Cell Lysis Buffer

Guide-to-Cell-Proliferation-and-Apoptosis-Methods

Chapter 1: Cell Death - Apoptosis and Necrosis1.1Introduction21.1.1Terminology of cell death21.1.2Differences between necrosis and apoptosis31.1.3Apop

The-TRC-shRNA-Design-Methods-and-Rules

OverviewWe design shRNA molecules with an algorithm. Our algorithm uses several criteria to rank potential 21mer targets within each human and mouse R

The-Fungal-Genetics-Stock-Center-Methods

Some basic Neurospora methods compiled at StanfordVogel's Minimal MediumD. D. Perkins - Hints for the care, feeding and breeding of NeurosporaStra

Tissue-Culture-Methods1

I. TYPES OF CELLS GROWN IN CULTURETissue culture is often a generic term that refers to both organ culture and cell culture and the terms are often us

COMPARISION-OF-DIFFERENT-PROTEIN-DETERMINATION-METHODS

COMPARISION OF DIFFERENT PROTEIN DETERMINATION METHODSCompanyMethodDetection  RangeApplications -CompatibilityAssay protocolPrecautions-InterferencesA

Tissue-Culture-Methods2

IV. MAINTENANCECultures should be examined daily, observing the morphology, the color of the medium and the density of the cells. A tissue culture log

《Nature-Methods》大脑地图图解

  多年来,出现了多种“大脑地图”,每一种都关注不同的大脑过程,从新陈代谢到认知功能。虽然这些地图很重要,但单独使用它们会限制研究人员从中得出的发现。  现在,来自蒙特利尔神经学研究所的一个团队和其他研究人员在一个地方汇集了40多张现有的大脑地图。这个被称为神经图谱的数据库有望帮助科学家发现不同大脑

Tissue-Culture-Methods3

REFERENCES:R. Ian Freshney, Culture of Animal cells: A manual of basic techniques, Wiley-Liss, 1987.VI. TISSUE CULTURE PROCEDURESEach student should m